Patient Centered Postpartum Contraception App

Contraceptive Usage Clinical Trial

Official title: Patient Centered Postpartum Contraception App

Status Completed

Clinical Trial Summary

This study will evaluate a smart phone-based application ("app") designed to inform pregnant women ages 15-25 about their contraception options. The goal of this research will be to evaluate the usability, feasibility and acceptability of this app.

Clinical Trial Description

This study will evaluate a smart phone-based application ("app") designed to inform pregnant women ages 15-25 about their contraception options. The goal of this research will be to evaluate the usability, feasibility and acceptability of this app. Participants will be asked to complete a survey after informed consent and before using the app. After using the app, participants will complete a second survey. This second survey will ask questions about the app including the following topics: Usability, user-friendliness, navigation, user interface, time spent, organization readability; Feasibility, informative, helpful, comprehensible, quality of art, interface, sound; and Acceptability breadth of content, depth of content, engaging and motivating, Innovative utility and value. Women will also rate the degree to which they promote use of the product: would use the app if available, believe the app will support contraceptive use and would recommend the app to peers. Study participation will end once participants are done with the second survey. ;

Related Conditions & MeSH terms

• Contraceptive Usage

• NCT number: NCT03402217
• Study type: Observational
• Source: University of Chicago
• Status: Completed
• Start date: May 18, 2018
• Completion date: January 7, 2019